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Impact of environmental tobacco smoke on the incidence of mutations in epidermal growth factor receptor gene in never-smoker patients with non-small-cell lung cancer.

Authors
 Young Joo Lee  ;  Byoung Chul Cho  ;  Sun Ha Jee  ;  Jin Wook Moon  ;  Se Kyu Kim  ;  Joon Chang  ;  Kyung Young Chung  ;  In Kyu Park  ;  Sung Ho Choi  ;  Joo-Hang Kim 
Citation
 JOURNAL OF CLINICAL ONCOLOGY, Vol.28(3) : 487-492, 2010 
Journal Title
 JOURNAL OF CLINICAL ONCOLOGY 
ISSN
 0732-183X 
Issue Date
2010
MeSH
Adult ; Aged ; Aged, 80 and over ; Carcinoma, Non-Small-Cell Lung/epidemiology ; Carcinoma, Non-Small-Cell Lung/etiology* ; Carcinoma, Non-Small-Cell Lung/genetics ; Female ; Humans ; Incidence ; Lung Neoplasms/epidemiology ; Lung Neoplasms/etiology* ; Lung Neoplasms/genetics ; Male ; Middle Aged ; Mutation ; Receptor, Epidermal Growth Factor/genetics* ; Tobacco Smoke Pollution
Abstract
PURPOSE: Active tobacco smoking has been associated with the incidence of epidermal growth factor receptor (EGFR) mutations. However, the impact of environmental tobacco smoke (ETS) on EGFR mutations has been unknown. We investigated an association between ETS exposure and EGFR mutations in never smokers with non-small-cell lung cancer (NSCLC). PATIENTS AND METHODS: We enrolled 179 consecutive never smokers who were newly diagnosed with NSCLC. The history of ETS exposure was obtained with a standardized questionnaire that included exposure period, place, and duration. The nucleotide sequences of exons 18 to 21 on EGFR gene were determined using nested polymerase chain reaction amplification. RESULTS: The incidence of EGFR mutations was significantly lower in patients with ETS exposure than in those without (38.5% v 61.4%; P = .008). In a logistic regression model that adjusted for sex and histology, an adjusted odds ratio (AOR) for the risk of EGFR mutations with exposure to ETS was 0.40 (95% CI, 0.20 to 0.81; P = .011). In quartile groups based on total smoker-year, the AORs for the lowest- to highest-quartile groups were 0.59 (95% CI, 0.23 to 1.49), 0.50 (95% CI, 0.17 to 1.50), 0.48 (95% CI, 0.20 to 1.18), and 0.22 (95% CI, 0.08 to 0.62; P(trend) = .028). Among the types of ETS exposure, adulthood ETS and household ETS were significantly associated with the incidence of EGFR mutations. Patients with ETS exposure showed a lower response rate to EGFR tyrosine kinase inhibitors than did patients without ETS exposure (24.6% v 44.8%; P = .053). CONCLUSION: ETS exposure is negatively associated with EGFR mutations in never smokers with NSCLC
Full Text
http://jco.ascopubs.org/content/28/3/487.long
DOI
10.1200/JCO.2009.24.5480
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
4. Graduate School of Public Health (보건대학원) > Graduate School of Public Health (보건대학원) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Thoracic and Cardiovascular Surgery (흉부외과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Se Kyu(김세규)
Kim, Joo Hang(김주항)
Moon, Jin Wook(문진욱)
Park, In Kyu(박인규)
Lee, Young Joo(이영주)
Chang, Joon(장준) ORCID logo https://orcid.org/0000-0003-4542-6841
Chung, Kyung Young(정경영)
Cho, Byoung Chul(조병철) ORCID logo https://orcid.org/0000-0002-5562-270X
Jee, Sun Ha(지선하) ORCID logo https://orcid.org/0000-0001-9519-3068
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/100403
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